Vector Oncology, an affiliate of ConcertAI, 6555 Quince, Suite 400, Memphis, TN 38119, USA.
Pfizer Inc., 235 East 42nd Street, NY 10017, USA.
Future Oncol. 2021 Mar;17(9):1001-1011. doi: 10.2217/fon-2020-0744. Epub 2020 Nov 10.
Limited studies have evaluated palbociclib-based therapy use in patients with advanced/metastatic breast cancer in the real world. This retrospective study used medical records from US community oncology practices to address the gap. Eligible patients receiving palbociclib-based therapy per label indication from 3 February 2015 to 31 December 2017 were included. Descriptive analyses were conducted for patient characteristics, treatment patterns and clinical outcomes. The study included 233 patients who received palbociclib + aromatase inhibitor (P+AI) and 48 who received palbociclib + fulvestrant (P+F). Real-world progression-free rate for P+AI was 69.8% (46.8%) at 12 (24) months (P+F: 43.5% [39.9%]) months. Real-world survival rate was 89.8% (71.4%) at 12 (24) months (P+F: 76.3% [65.0%]). The study findings are consistent with previous studies of palbociclib-based therapy.
有限的研究评估了帕博西尼为基础的治疗在真实世界中的晚期/转移性乳腺癌患者中的应用。这项回顾性研究使用了美国社区肿瘤学实践的病历来填补这一空白。符合条件的患者根据标签指示接受帕博西尼为基础的治疗,时间为 2015 年 2 月 3 日至 2017 年 12 月 31 日。对患者特征、治疗模式和临床结果进行了描述性分析。该研究包括 233 名接受帕博西尼+芳香酶抑制剂(P+AI)治疗的患者和 48 名接受帕博西尼+氟维司群(P+F)治疗的患者。P+AI 的真实无进展率为 12(24)个月时的 69.8%(46.8%)(P+F:43.5%[39.9%])。12(24)个月时的真实生存率为 89.8%(71.4%)(P+F:76.3%[65.0%])。研究结果与之前的帕博西尼为基础的治疗研究一致。